USP48 Polyclonal Antibody, 100ul Cell Culture Plates Defects in this gene are

Defects in this gene are a cause of Zellweger syndrome (ZWS)

An important paralog of this gene is ZNF718

and their presence on the polysomes

The receptor mediates cell contraction and proliferation

This encoded protein could play an important role in the pathogenesis of Alzheimer's disease

USP48 Polyclonal Antibody, 100ul Cell Culture Plates Defects in this gene areUSP48 (ubiquitin specific peptidase 48) encodes a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly ubiquitin precursors as well as that of ubiquitinated